BEUDAMED
    35 results · 31ms · Sources: EU EUDAMED, US FDA

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    ADAPTERS WITH X-COATING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KALORE™

    FDA UDI
    Gc America Inc.·14548161291194·KALORE™ Unitips (0.16 mL/0.3 g) Box of 10 uniti...

    KALORE™

    FDA UDI
    Gc America Inc.·D0470036041·KALORE™ Unitips (0.16 mL/0.3 g) Box of 10 uniti...

    Sperm-TIC 1:20

    FDA UDI
    BIOANALYTIC GmbH, biomed. Analysentechnik·04061609000019·For microscopic counting of Sperms. (5 Tests)

    Sperm-TIC 1:20 plus

    FDA UDI
    BIOANALYTIC GmbH, biomed. Analysentechnik·04061609000026·For microscopic counting of Sperms. (100 Tests)

    Bionet

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935109228·

    NATURE'S CHEMIST PAIN RELIEF OINTMENT AND THERAPEUTIC ULTRASOUND COUPLING AGENT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    DANA DIABECARE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Signature Femoral Head

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215095567·

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·July 21, 2016

    JAW INS.BIP.MACRO FORCEPS D: 5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG TUTTLINGEN 78532·Product code GEI·December 12, 2014

    LIFEPAK 12 PHYSIO CONTROL

    FDA Adverse Event
    Death ·PHYSIO CONTROL·Product code LDD·June 11, 2001

    BIPOLAR MACRO FORCEPS D:5/ 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    JAW INS. BIP. MARYLAND DISS. FCPS 5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·January 14, 2015

    BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

    JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

    MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·October 25, 2016

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015